TITERTEK MICROPLATE INCUBATOR
K-Number: K812340 · 1981-09-23
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Device Summary
Frequently Asked Questions
What is the TITERTEK MICROPLATE INCUBATOR?
TITERTEK MICROPLATE INCUBATOR is a medical device that received FDA 510(k) clearance on 1981-09-23. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K812340.
When did TITERTEK MICROPLATE INCUBATOR receive FDA 510(k) clearance?
TITERTEK MICROPLATE INCUBATOR received FDA 510(k) clearance on 1981-09-23, under 510(k) number K812340.
Who is the listed applicant for TITERTEK MICROPLATE INCUBATOR?
The FDA 510(k) record lists Flow Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TITERTEK MICROPLATE INCUBATOR?
The FDA product code for TITERTEK MICROPLATE INCUBATOR is JTQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Flow Laboratories, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JTQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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